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U.S. Department of Health and Human Services

Product Classification

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Device antiserum, fluorescent, chlamydia trachomatis
Regulation Description Chlamydia serological reagents.
Regulation Medical Specialty Microbiology
Review Panel Microbiology
Product CodeLJP
Premarket Review Division of Microbiology Devices (DMD)
Division of Microbiology Devices (DMD)
Submission Type 510(k)
Regulation Number 866.3120
Device Class 1
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting
Eligible
Implanted Device? No
Life-Sustain/Support Device? No
Third Party Review
Accredited Persons
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